*Position: Project Manager * *Location: Groton, CT / Peapack, NJ / Collegeville, PA*
*Duration: 12 Months* *Summary:* The Project Manager (PM) will manage the integration plans (e.g., deliverables, risks, issues) for Regulatory, Content management, Clinical Trials, Safety and Centralized Services Integration activities. PM will be deeply involved in improving the consistency, predictability and efficiency of the program delivery capability. The PM must also ensure that the operational issues of the integrations are managed, focusing on the project interface with project leaders, project teams, integration tem *Responsibilities:* • Overlook Information Management Acquisitions, Collaborations and Divestures (ACD) projects/programs execution • Define and manage plans and timelines • Risk management, including risk assessment for the overall program • Ensure proper execution of the risk plan throughout the projects lifecycle • Perform data mapping from source to target systems • Lead a geographically distributed team • Manage and deploy initiatives by influence *Key Deliverables: * • Integrated project plan for the program • Status reports • Communication decks • Communication Plan • Data migration/transfer plans • Product Template (includes Product and study data) • Cross functional dependency plan • Manage SharePoint meeting space • Create and manage Risk register *Skills: * • Must possess extensive knowledge and expertise in program/project management, portfolio management, and integrations • Understand Clinical, Safety, Regulatory and Content Management systems and processes • Migration Analysis and Documentation • Bachelors or Master’s Degree • 10-15 years of Integration and business/industry work experience • Minimum of 5 years of program/project management experience • 3-5 years of equivalent leadership experience *Tools and Technologies: * • Clinical: EDC (e.g. Oracle Clinical), Registry (e.g. RTII), Analysis and Reporting (CDARS) • Regulatory: Product and Licensing (e.g. PEARL), Submissions (e.g. eCTD) • Content Management: Document Management (e.g. GDMS) • Safety: Pharmacovigilance System (e.g. ARGUS) *Thanks & Regards* *Ajeet Dwivedi* (IT Recruiter) Email: ajeet.dwiv...@nityo.com -- You received this message because you are subscribed to the Google Groups "USITCV" group. To unsubscribe from this group and stop receiving emails from it, send an email to usitcv+unsubscr...@googlegroups.com. To post to this group, send email to usitcv@googlegroups.com. Visit this group at https://groups.google.com/group/usitcv. For more options, visit https://groups.google.com/d/optout.
